Quality Officer, GLP/ GMP

Capio Spine Center Stockholm; Bradford; On-site; GBP 32,000; Full time

Job summary

An established industry player is seeking a Quality Officer to enhance their QA team at the Bradford site. This role presents an exciting opportunity for career growth, focusing on GMP and GLP compliance within analytical laboratories. The successful candidate will support the Quality Manager, maintain the Quality Management System, and ensure adherence to quality standards. If you have a degree in a scientific field or substantial QA experience, along with strong IT and interpersonal skills, this position could be the perfect fit for you. Join a dynamic team dedicated to excellence in quality assurance.

Qualifications

• Degree in a relevant Scientific/STEM subject or significant QA experience.
• Experienced in quality/QMS duties within a GLP/GMP framework.

Responsibilities

• Support quality activities and maintain the Quality Management System.
• Train personnel in GMP, GLP, and related QMS requirements.
• Perform audits and inspections, reporting deficiencies.

Skills

Quality Management System (QMS)

GMP

GLP

CAPA

Documentation Review

Interpersonal Skills

Report Writing

Education

Degree in Scientific/STEM subject

Tools

IT Literacy

Job description

Join to apply for the Quality Officer, GLP/ GMP role at Capio Spine Center Stockholm.

Type: Permanent
Location: Bradford (fully onsite)
Hours: Days
Salary: CIRCA £32,000

Our client, a multi-sited GMP/GLP testing company, is growing their QA team and looking to recruit a QA Officer to join their specialized QA team.

This role offers an exciting opportunity for career development. Supporting the Quality Manager, the successful candidate will work with the Quality team and Analytical Scientists at the Bradford site to implement, maintain, and improve procedures and processes that ensure GMP and GLP compliance within the analytical laboratory areas.

The Role

• Supporting the quality activities of the laboratory areas.
• Maintaining & improving the Quality Management System (QMS).
• Training personnel in GMP, GLP, and related QMS requirements.
• Supporting completion of action plans from regulatory/customer audits.
• Maintaining and executing the internal audit schedule.
• Managing the Supplier oversight programme.
• Performing audits and inspections, reporting deficiencies to the Quality Manager and Operations Director, covering facilities, equipment, systems, procedures, records, data, and information.
• Reviewing and approving production and analytical documentation, including Certificates of Analysis.
• Ensuring document control systems are maintained.
• Investigating non-conformances, deviations, OOS, and supporting CAPAs and customer complaints.
• Assisting with or hosting audits by customers and regulatory bodies.

The Person

• Holds a degree in a relevant Scientific/STEM subject or has significant QA (GLP/GMP) experience.
• Experienced in quality/QMS duties such as CAPA, deviations, documentation review within a GLP/GMP framework.
• Strong IT literacy.
• Excellent interpersonal and report-writing skills.

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